CAS 65053-26-1
:N-(pyridin-4-yl)benzene-1,2-diamine
Description:
N-(pyridin-4-yl)benzene-1,2-diamine, with the CAS number 65053-26-1, is an organic compound characterized by its dual amine functional groups and a pyridine ring. This compound features a benzene backbone substituted with an amino group at the 1 and 2 positions, and a pyridine moiety at the N-position of one of the amines. It typically appears as a solid at room temperature and is soluble in polar organic solvents. The presence of both amine and pyridine functionalities suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as these groups can participate in hydrogen bonding and coordination with metal ions. Additionally, the compound may exhibit interesting electronic properties due to the conjugation between the aromatic systems. Its reactivity can be influenced by the basicity of the amine groups and the electron-withdrawing nature of the pyridine ring, making it a candidate for various chemical reactions, including coupling reactions and ligand formation in coordination chemistry.
Formula:C11H11N3
InChI:InChI=1/C11H11N3/c12-10-3-1-2-4-11(10)14-9-5-7-13-8-6-9/h1-8H,12H2,(H,13,14)
SMILES:c1ccc(c(c1)N)N=c1cc[nH]cc1
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Found 4 products.
4-(2-Aminoanilino)pyridine
CAS:Controlled Product<p>Applications An intermediate used to prepare Timiperone as well as cyclooxygenase-2 inhibitors and adrenergic agents<br>References Eftink, M.R., et al.: J. Phys. Chem., 99, 5713 (1995), Palmer, B.D., et al.: J. Med. Chem., 41, 5457 (1998), Pinto, I., et al.: J. Med. Chem., 51, 7205 (2008),<br></p>Formula:C11H11N3Color and Shape:NeatMolecular weight:185.234-(2-Aminoanilino)pyridine
CAS:<p>4-(2-Aminoanilino)pyridine is a pyridine that has been shown to be an impurity in the acid salt of 4-(2-aminophenyl)pyridine. It is an acidified impurity that can form when the pyridine reacts with hydrochloric acid or sulfuric acid.</p>Formula:C11H11N3Purity:Min. 95%Color and Shape:PowderMolecular weight:185.23 g/mol



